Canonical Allele Identifier: PA2825644310
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp2472Val
CA048153
NM_001127511.3:c.7415A>T